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Characterization of adenosine receptors in bovine chondrocytes and fibroblast-like synoviocytes exposed to low frequency low energy pulsed electromagnetic fields.

机译:牛软骨细胞和腺癌中腺苷受体的表征  暴露于低频低能脉冲电磁场​​的成纤维细胞样滑膜细胞。

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摘要

Objective: The present study describes the presence and binding parameters of the A1, A2A, A2B and A3 adenosine receptors in bovinechondrocytes and fibroblast-like synoviocytes. The effect of low frequency low energy pulsed electromagnetic fields (PEMFs) on the adenosinereceptor affinity and density was studied.Methods: Saturation, competition binding experiments and Western blotting assays in the absence and in the presence of PEMFs on theadenosine receptors in bovine chondrocytes or fibroblast-like synoviocytes were performed. Thermodynamic analysis of the A2A or A3 bindingwas studied to investigate the forces driving drugereceptor coupling. In the adenylyl cyclase and proliferation assays the potency of typicalhigh-affinity A2A or A3 agonists in the absence and in the presence of PEMFs was evaluated.Results: Bovine chondrocytes and fibroblast-like synoviocytes expressed all adenosine receptors. PEMFs evoked an up-regulation of A2A andA3 receptors and thermodynamic parameters indicate that adenosine binding is enthalpy and entropy driven. In PEMF-treated cells thepotency of typical A2A or A3 agonists on cyclic AMP assays was significantly increased when compared with the untreated cells. PEMFspotentiated the effect of A2A or A3 agonists on cell proliferation in both cell types.Conclusions: PEMFs mediate an up-regulation of A2A and A3 receptors related to an increase of their functional activities in bovine chondrocytesand fibroblast-like synoviocytes. No differences are present in adenosine affinity and in the drugereceptor interactions. Our data couldbe used as a trigger to future studies addressed to PEMFs and adenosine therapeutic intervention in inflammatory joint diseases.
机译:目的:本研究描述了牛软骨细胞和成纤维样滑膜细胞中A1,A2A,A2B和A3腺苷受体的存在及其结合参数。研究了低频低能脉冲电磁场​​(PEMF)对腺苷受体亲和力和密度的影响。方法:在无或存在PEMFs的条件下,对牛软骨细胞或成纤维细胞中腺苷受体进行饱和,竞争结合实验和蛋白质印迹分析样滑膜细胞被执行。研究了A2A或A3结合的热力学分析,以研究驱动药物受体耦合的力。在腺苷酸环化酶和增殖试验中,评估了在不存在和存在PEMF的情况下典型的高亲和力A2A或A3激动剂的效力。结果:牛软骨细胞和成纤维细胞样滑膜细胞表达了所有腺苷受体。 PEMF引起A2A和A3受体的上调,并且热力学参数表明腺苷结合是焓和熵驱动的。与未经处理的细胞相比,在经PEMF处理的细胞中,典型的A2A或A3激动剂在环AMP分析中的效能显着提高。 PEMF增强了A2A或A3激动剂对两种细胞类型的细胞增殖的影响。结论:PEMF介导A2A和A3受体的上调与它们在牛软骨细胞和成纤维细胞样滑膜细胞中的功能活性增加有关。腺苷亲和力和药物受体相互作用没有差异。我们的数据可用于引发针对炎症性关节疾病的PEMF和腺苷治疗性干预的未来研究。

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